Duckworth & Kent, Ltd. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
FDA 510(k) Regulatory Record - Duckworth & Kent, Ltd. Ophthalmic ✕
6 devices
Cleared
Oct 23, 2008
DUCKWORTH & KENT, LTD., IMPLANTATION SYSTEM, MODEL DK7786
Ophthalmic
160d
Cleared
Jun 20, 2008
DUCKWORTH & KENT LTD INJECTOR, MODEL: DK7797-2
Ophthalmic
241d
Cleared
May 22, 2006
DUCKWORTH & KENT LTD LENS DELIVERY SYSTEM, MODEL DK7788
Ophthalmic
41d
Cleared
Jan 30, 2006
DUCKWORTH & KENT LTD CARTRIDGE LENS DELIVERY SYSTEM, MODEL DK7797
Ophthalmic
77d
Cleared
Dec 28, 2004
CAPSULE TENSION RING INSERTER, MODEL 7-810
Ophthalmic
106d
Cleared
Oct 06, 2003
DUCKWORTH & KENT LTD LENS DELIVERY SYSTEM
Ophthalmic
300d